An STD Prevention Intervention for Men Newly Released From Jail

This study has been completed.
Sponsor:
Collaborator:
STAND, Inc.
Information provided by:
Centers for Disease Control and Prevention
ClinicalTrials.gov Identifier:
NCT00260780
First received: December 1, 2005
Last updated: NA
Last verified: December 2005
History: No changes posted
  Purpose

Study participants who are exposed to the intervention will: 1)report more condom use during sexual episodes; 2) have fewer new and repeat STD infections 3)demonstrate greater risk reduction, communication, and anger management skills; 4) report fewer substance use behaviors, and 5)report more health care seeking activities, than the participants in the control group


Condition Intervention
Sexually Transmitted Diseases
Risk Behavior
Behavioral: The MISTERS Intervention for Post Jail Release Men

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Factorial Assignment
Masking: Open Label
Primary Purpose: Prevention
Official Title: The MISTERS Project: An STD Prevention Intervention for Men Newly Released From Jail

Resource links provided by NLM:


Further study details as provided by Centers for Disease Control and Prevention:

Primary Outcome Measures:
  • Change in risk behaviors

Secondary Outcome Measures:
  • Reported STDs

Estimated Enrollment: 300
Study Start Date: June 2001
Estimated Study Completion Date: June 2004
Detailed Description:

The MISTERS study is a randomized control trial of a cognitive-behavioral skill building multi-session intervention that targets men who are newly released from jail and have a history of drug use. Men 45 days or less post release with self reported HIV negative and substance use histories were randomized into either a 5-session intervention or control group. Study participation included four time-sensitive interviews and STD testing at three time periods. The interview questions included demographics, STD history and knowledge, sexual risk behaviors, as well as an assessment of anger management, communication, and condom use skills.

  Eligibility

Ages Eligible for Study:   18 Years to 60 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • ages 18 to 60, English speaking, not in jail for sexual offenses (rape or child molestation), reported risk behavior in two months prior to incarceration, weekday and evening availability, viable contact information, self-reported HIV negative status, released from jail no more than 45 days prior, and not visibly under the influence of drugs or alcohol at the time of eligibility determination

Exclusion Criteria:

  • Opposite of the above
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00260780

Locations
United States, Georgia
STAND, Inc.
Decatur, Georgia, United States, 30335
Sponsors and Collaborators
STAND, Inc.
Investigators
Study Chair: Samantha P Williams, Ph.D. CDC/NCHSTP/DSTDP/BIRB
Principal Investigator: Charles Sperling, M.S. STAND, Inc.
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00260780     History of Changes
Other Study ID Numbers: CDC-NCHSTP-3728, U52/CCU422491, H25/CCH404332-11
Study First Received: December 1, 2005
Last Updated: December 1, 2005
Health Authority: United States: Federal Government

Keywords provided by Centers for Disease Control and Prevention:
sexually transmitted diseases
Risk Behavior

Additional relevant MeSH terms:
Sexually Transmitted Diseases
Infection
Virus Diseases
Genital Diseases, Male
Genital Diseases, Female

ClinicalTrials.gov processed this record on July 22, 2014